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"HELY AND WEBER" Limb orthosis (Non-Sterile) - Taiwan Registration edd2b433856430d86c35ad613a93b1bb

Access comprehensive regulatory information for "HELY AND WEBER" Limb orthosis (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number edd2b433856430d86c35ad613a93b1bb and manufactured by HELY AND WEBER. The authorized representative in Taiwan is ORTHOHEALTH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HELY AND WEBER, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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edd2b433856430d86c35ad613a93b1bb
Registration Details
Taiwan FDA Registration: edd2b433856430d86c35ad613a93b1bb
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Device Details

"HELY AND WEBER" Limb orthosis (Non-Sterile)
TW: "่ตซ่މๅ‰ไผฏ" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

edd2b433856430d86c35ad613a93b1bb

Ministry of Health Medical Device Import No. 020112

DHA09402011209

Company Information

United States

Product Details

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Feb 21, 2019

Feb 21, 2024

Cancellation Information

Logged out

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